A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5952944



Internal ID22728241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:90315095..90315095hg38UCSC Ensembl
chr7:89944409..89944409hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg38775
hg19775
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17434684
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5952944
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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